2011
DOI: 10.1016/j.ijrobp.2009.12.045
|View full text |Cite
|
Sign up to set email alerts
|

Acute and Late Toxicity in a Randomized Trial of Conventional Versus Hypofractionated Three-Dimensional Conformal Radiotherapy for Prostate Cancer

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2
1

Citation Types

8
100
1
1

Year Published

2012
2012
2019
2019

Publication Types

Select...
5
3

Relationship

0
8

Authors

Journals

citations
Cited by 142 publications
(110 citation statements)
references
References 32 publications
8
100
1
1
Order By: Relevance
“…In this scenario, even though the OAR receives dose equivalent to the tumor dose ( the model predicts that hypofractionation will be preferable over multi-fractionation. This is consistent with recently published randomized trials where hypofractionated radiotherapy was better than conventional radiotherapy for prostate cancer (26,27). Previous radiobiological models predicted that hypofractionation is optimal for prostate cancer based on the fact that 0 0   is larger than…”
Section: Resultssupporting
confidence: 90%
“…In this scenario, even though the OAR receives dose equivalent to the tumor dose ( the model predicts that hypofractionation will be preferable over multi-fractionation. This is consistent with recently published randomized trials where hypofractionated radiotherapy was better than conventional radiotherapy for prostate cancer (26,27). Previous radiobiological models predicted that hypofractionation is optimal for prostate cancer based on the fact that 0 0   is larger than…”
Section: Resultssupporting
confidence: 90%
“…Benign PSA bounces were common with 33.3% of all patients. The median time to PSA bounce was 13 months (range, [6][7][8][9][10][11][12][13][14][15][16][17][18]. The median height of PSA bounce was 0.34 ng/mL (range, 0.21-1.39).…”
Section: Resultsmentioning
confidence: 99%
“…The hypofractionated radiotherapy schema may improve the biochemical control of prostate cancer without increasing toxicities associated with late-responding tissue (8) . One phase III study trial suggested that hypofractionation regiment of 62 Gy in fractions is safe and acute and late complication were equivalent to that of the conventional fractionated regimen of 80 Gy in 40 fractions (10) .…”
Section: Introductionmentioning
confidence: 99%
“…26 Arcangeli et al used high dose EBRT in both groups but only included high-risk PC patients and had a limited follow-up time (median 33,5 months). 27 In contrast Lukka et al reported a 7% difference in biochemical or clinical failure favoring patients treated with a dose of 66 Gy in 33 fractions compared to the hypofractionated group who received 52,5 Gy in 20 fractions. 28 These poor results, however, can be explained by the low dose given in both groups.…”
Section: Hypofractionation In the Primary Setting For Pcmentioning
confidence: 93%
“…30 No significant differences in late toxicity are reported, although acute GI and GU toxicity seems to develop earlier in hypofractionated than in conventionally fractionated EBRT. 27 High dose hypofractionated EBRT has shown promising results, although long-term biochemical and clinical outcome and late toxicity reports are eagerly awaited. Furthermore, the ideal fractionation schemes are yet to be determined.…”
Section: Hypofractionation In the Primary Setting For Pcmentioning
confidence: 99%